In vitro fertilization outcome triggered with different dosage of GnRH and hCG in antagonist protocol
Phase 2
Recruiting
- Conditions
- infertility patients going ivf.Female infertility
- Registration Number
- IRCT20160130026260N2
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 108
Inclusion Criteria
18-40 years women
Follicular stimulating hormone lower than 12U/lit
menstruation interval 25-34days
Having both ovaries
infertile women
Exclusion Criteria
Endocrine disease
uterine anomaly
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical pregnancy rate. Timepoint: 2 months after embryo transfer. Method of measurement: Ultrasonography.
- Secondary Outcome Measures
Name Time Method